Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
Frequency and complexity of de novo structural mutation in autism.
Stability and change in autism spectrum disorder diagnosis from age 3 to middle childhood in a high-risk sibling cohort.
Enhanced social attention in female infant siblings at risk for autism.
Genome sequencing of autism-affected families reveals disruption of putative noncoding regulatory DNA.
Defining the effect of the 16p11.2 duplication on cognition, behavior, and medical comorbidities.
The number of genomic copies at the 16p11.2 locus modulates language, verbal memory, and inhibition.
The discovery of integrated gene networks for autism and related disorders.
The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.
Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
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